The DOI matches its Crossref record; 52 of the 52 references it cites were found in a registry or an index.
Chronic Stress Induces Contrasting Patterns of Dendritic Remodeling in Hippocampal and Amygdaloid Neurons
Open accessAbstract
The hippocampus and the amygdala are essential components of the neural circuitry mediating stress responses. The hippocampus, which provides negative feedback regulation of the stress response, is particularly vulnerable to degenerative changes caused by chronic stress. Unlike the hippocampus, relatively little is known about how stress affects the amygdala and the nature of its role in the stress response. Hence, we examined the effects of two different models of chronic stress on hippocampal and amygdaloid neuronal morphology in rats. In agreement with previous reports, chronic immobilization stress (CIS) induced dendritic atrophy and debranching in CA3 pyramidal neurons of the hippocampus. In striking contrast, pyramidal and stellate neurons in the basolateral complex of the amygdala exhibited enhanced dendritic arborization in response to the same CIS. Chronic unpredictable stress (CUS), however, had little effect on CA3 pyramidal neurons and induced atrophy only in BLA bipolar neurons. These results indicate that chronic stress can cause contrasting patterns of dendritic remodeling in neurons of the amygdala and hippocampus. Moreover, CIS, but not CUS, reduced open-arm activity in the elevated plus-maze. These findings raise the possibility that certain forms of chronic stress, by affecting specific neuronal elements in the amygdala, may lead to behavioral manifestations of enhanced emotionality. Thus, stress-induced structural plasticity in amygdala neurons may provide a candidate cellular substrate for affective disorders triggered by chronic stress.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In the basolateral amygdala (BLA) chronic unpredictable stress also produced dendritic atrophy but chronic immobilization stress instead increased dendritic branching (Banasr and Duman, 2007;Vyas et al, 2002Vyas et al, , 2003)).”
From Neurocircuitry of Mood Disorders (2010) · cites this paper as Vyas et al, 2002
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In animals, chronic stress results in the prolonged release of glucocorticoids and leads to hypertrophy of the amygdala and nucleus accumbens, atrophy of the hippocampus and prefrontal cortex (PFC), and functional impairment of the PFC (44–55).”
From Psychedelics and Other Psychoplastogens for Treating Mental Illness. (2021) · cites this paper as [47]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“enhanced BDNF/TrkB signaling in the amygdala leads to maladaptive plasticity resulting in overactivation of this brain region and exacerbated anxiety and fear responses (47, 198–200)”
From Psychedelics and Other Psychoplastogens for Treating Mental Illness. (2021) · cites this paper as [47]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“By contrast to the PFC and hippocampus, dendrites in the amygdala expand in response to chronic stress exposure112.”
From Stress signalling pathways that impair prefrontal cortex structure and function (2009) · cites this paper as [112]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In contrast to the PFC, chronic stress exposure increases dendritic growth in the amygdala77, thus accentuating the imbalance of amygdala over PFC function.”
From Stress weakens prefrontal networks: molecular insults to higher cognition (2015) · cites this paper as [77]
Experimental — accuracy not yet measured
The cited source says what the claim attributes to it.
In the citing paper
“In the basolateral amygdala (BLA) chronic unpredictable stress also produced dendritic atrophy but chronic immobilization stress instead increased dendritic branching (Banasr and Duman, 2007;Vyas et al, 2002Vyas et al, , 2003)).”
From Neurocircuitry of Mood Disorders (2010) · cites this paper as Vyas et al, 2002
The cited source says what the claim attributes to it.
In the citing paper
“The authors revealed that chronic immobilisation stress in rats resulted in significant dendritic atrophy of apical and basal dendrites of CA3 pyramidal neurons, with a more pronounced loss in apical dendrites.”
From Chronic Stress-Associated Depressive Disorders: The Impact of HPA Axis Dysregulation and Neuroinflammation on the Hippocampus—A Mini Review (2025) · cites this paper as [95]
The cited source says what the claim attributes to it.
In the citing paper
“Animal studies revealed that chronic stress causes atrophy of apical dendrites of pyramidal neurons in the CA3 region of the hippocampus (Magarinos et al. 1996; Vyas et al. 2002; Watanabe et al. 1992).”
From Neurotrophic factors and neuroplasticity pathways in the pathophysiology and treatment of depression (2018) · cites this paper as Vyas et al. 2002
The cited source says what the claim attributes to it.
In the citing paper
“This view is supported by recent evidence that individual brain regions are affected by stress in very different ways.”
From Episodic memory, perceptual memory, and their interaction: Foundations for a theory of posttraumatic stress disorder. (2014) · cites this paper as Vyas, Mitra, Rao, & Chattarji, 2002
The cited source says what the claim attributes to it.
In the citing paper
“a study of neuronal morphology showed that the same stress experience produced dendritic atrophy and debranching in the hippocampus at the same time as producing enhanced dendritic arborization in the amygdala”
From Episodic memory, perceptual memory, and their interaction: Foundations for a theory of posttraumatic stress disorder. (2014) · cites this paper as Vyas, Mitra, Rao, & Chattarji, 2002
In the citing paper
“In rodents, repeated stress results in dendritic atrophy and reduced glial cell counts in hippocampal regions (McEwen and Magarinos, 2001) as well as increased dendritic branching in the basolateral amygdala (Vyas et al., 2002).”
From Individual differences in amygdala-medial prefrontal anatomy link negative affect, impaired social functioning, and polygenic depression risk (2012) · cites this paper as Vyas et al., 2002
In the citing paper
“Specifically, studies of rodents show that stress increases dendritic arborization and spine density of the amygdala, with concomitant increases in anxiety-like behaviors (Vyas et al., 2002; Vyas et al., 2003, Mitra et al., 2005).”
From The impact of developmental timing for stress and recovery (2015) · cites this paper as Vyas et al., 2002
In the citing paper
“In contrast, stress-induced amygdala morphology and volume changes seem to persist (Vyas et al., 2002, Adamec et al., 2005, Tottenham et al., 2010).”
From The impact of developmental timing for stress and recovery (2015) · cites this paper as Vyas et al., 2002
In the citing paper
“By contrast, stress results in atrophy of the hippocampus and medial PFC (mPFC) (Magariños et al., 1997, Vyas et al., 2002, Radley et al., 2006).”
From The impact of developmental timing for stress and recovery (2015) · cites this paper as Vyas et al., 2002
In the citing paper
“Neuronal and synaptic remodeling in BLA PNs, along with enhanced glutamatergic transmission, has been repeatedly associated with the negative consequence of stress (14,33,34,40), and prevention of these changes is paralleled by a protection against stress-induced increases in anxiety-like behavior (26,41).”
From Chronic Stress Remodels Synapses in an Amygdala Circuit-Specific Manner (2019) · cites this paper as [14]
In the citing paper
“Repeated stress causes dendritic shortening in medial prefrontal cortex (Sousa et al., 2000; Wellman, 2001; Vyas et al., 2002; Kreibich and Blendy, 2004; Cook and Wellman, 2004; Radley et al., 2004; Brown et al., 2005; Radley et al., 2005)”
From Central effects of stress hormones in health and disease: understanding the protective and damaging effects of stress and stress mediators (2008) · cites this paper as Vyas et al., 2002
In the citing paper
“but produces dendritic growth in neurons in amygdala (Vyas et al., 2002)”
From Central effects of stress hormones in health and disease: understanding the protective and damaging effects of stress and stress mediators (2008) · cites this paper as Vyas et al., 2002
In the citing paper
“both acute and chronic stress also increases spine synapse formation in amygdala (Vyas et al., 2002)”
From Central effects of stress hormones in health and disease: understanding the protective and damaging effects of stress and stress mediators (2008) · cites this paper as Vyas et al., 2002
In the citing paper
“Acute stress induces spine synapses in the CA1 region of hippocampus98 and both acute and chronic stress also increases spine synapse formation in amygdala,95-99 but chronic stress decreases it in hippocampus.77”
From Protective and damaging effects of stress mediators: central role of the brain (2006) · cites this paper as [95]
In the citing paper
“Repeated stress causes dendritic shortening in medial prefrontal cortex.89-95 but produces dendritic growth in neurons in amygdala,95 as well as in orbitofrontal cortex.96”
From Protective and damaging effects of stress mediators: central role of the brain (2006) · cites this paper as [95]
In the citing paper
“Behavioral correlates of remodeling in the prefrontal cortex include impairment in attention set shifting, possibly reflecting structural remodeling in the medial prefrontal cortex.95”
From Protective and damaging effects of stress mediators: central role of the brain (2006) · cites this paper as [95]
In the citing paper
“Additionally, multiple studies have found that chronic stress results in an increase in dendritic arborization and spinogenesis on BLA pyramidal neurons, increasing their intrinsic excitability and afferent stimulation in a manner that correlates with heightened anxiety-like behavior [70–72].”
From Amygdala FAAH and anandamide: mediating protection and recovery from stress (2013) · cites this paper as [70]
In the citing paper
“Acute traumatic stressors were found to cause increased spine density on basolateral amygdale (BlA) neurons and chronic stress leads to the expansion of BlA dendrites.”
From Neurobiological and Systemic Effects of Chronic Stress (2017) · cites this paper as [18]
In the citing paper
“Chronic stress causes dendritic shrinkage not only in CA3 and dentate gyrus neurons of hippocampus but also in medial amygdala and mPFC, while dendrites in BlA and orbitofrontal cortex expand with chronic stress.”
From Neurobiological and Systemic Effects of Chronic Stress (2017) · cites this paper as [18]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
The role of the amygdala in fear and anxiety
Davis, M. (1992) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.15.030192.002033 · Cited by 2,357
Neurocircuitry of stress: central control of the hypothalamo–pituitary–adrenocortical axis
Herman, J. P., & Cullinan, W. E. (1997) · Trends in Neurosciences · doi:10.1016/s0166-2236(96)10069-2 · Cited by 2,270
STRESS AND HIPPOCAMPAL PLASTICITY
McEwen, B. S. (1999) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.22.1.105 · Cited by 2,087
Hippocampal atrophy in recurrent major depression
Sheline, Y. I., Wang, P. W., Gado, M. H., Csernansky, J. G., & Vannier, M. W. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.9.3908 · Cited by 1,932
JACOBSON, L., & SAPOLSKY, R. (1991) · Endocrine Reviews · doi:10.1210/edrv-12-2-118 · Cited by 1,739
Cortisol levels during human aging predict hippocampal atrophy and memory deficits
Lupien, S. J., de Leon, M., de Santi, S., Convit, A., Tarshish, C., Nair, N. P. V., Thakur, M., McEwen, B. S., Hauger, R. L., & Meaney, M. J. (1998) · Nature Neuroscience · doi:10.1038/271 · Cited by 1,653
(1995) · American Journal of Psychiatry · doi:10.1176/ajp.152.7.973 · Cited by 1,610
Intrinsic firing patterns of diverse neocortical neurons
Connors, B. W., & Gutnick, M. J. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90185-d · Cited by 1,440
Swanson, L. W., & Petrovich, G. D. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01265-x · Cited by 1,351
Bremner, J. D., Randall, P., Vermetten, E., Staib, L., Bronen, R. A., Mazure, C., Capelli, S., McCarthy, G., Innis, R. B., & Charney, D. S. (1997) · Biological Psychiatry · doi:10.1016/s0006-3223(96)00162-x · Cited by 1,283
Research works printed but not linked: 1
- [28]28. McDonald AJ (1992) Cell types and intrinsic connections of the amyg- dala. In: The amygdala (Aggleton JP, ed), pp 67-96. New York: Wiley.
Cited by
Sorted by citations
Items 201–300 of 1,000
Toward an Animal Model of Posttraumatic Stress Disorder
Siegmund, A., & Wotjak, C. T. (2006) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1364.025 · Cited by 201
Gestational Hypoxia and Developmental Plasticity
Ducsay, C. A., Goyal, R., Pearce, W. J., Wilson, S. M., Hu, X., & Zhang, L. (2018) · Physiological Reviews · doi:10.1152/physrev.00043.2017 · Cited by 208
Stress-induced structural remodeling in hippocampus: Prevention by lithium treatment
Wood, G. E., Young, L. T., Reagan, L. P., Chen, B., & McEwen, B. S. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0400208101 · Cited by 202
Lei, A. A., Phang, V. W. X., Lee, Y. Z., Kow, A. S. F., Tham, C. L., Ho, Y.-C., & Lee, M. T. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26072940 · Cited by 207
“The morphology of dendrites in the hippocampus, particularly in CA3 pyramidal neurons and dentate gyrus granule neurons, exhibited shrinkage in dendrite length, as well as branch point reduction, relative to the control [95].”
Zucchi, F. C. R., Yao, Y., Ward, I. D., Ilnytskyy, Y., Olson, D. M., Benzies, K., Kovalchuk, I., Kovalchuk, O., & Metz, G. A. S. (2013) · PLoS ONE · doi:10.1371/journal.pone.0056967 · Cited by 193
de Kloet, E. R., DeRijk, R. H., & Meijer, O. C. (2007) · Nature Clinical Practice Endocrinology & Metabolism · doi:10.1038/ncpendmet0403 · Cited by 193
Forray, M. I., & Gysling, K. (2004) · Brain Research Reviews · doi:10.1016/j.brainresrev.2004.07.011 · Cited by 191
Kallarackal, A. J., Kvarta, M. D., Cammarata, E., Jaberi, L., Cai, X., Bailey, A. M., & Thompson, S. M. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.2588-13.2013 · Cited by 181
Estrogen Promotes Stress Sensitivity in a Prefrontal Cortex-Amygdala Pathway
Shansky, R. M., Hamo, C., Hof, P. R., Lou, W., McEwen, B. S., & Morrison, J. H. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhq003 · Cited by 191
Understanding stress: Insights from rodent models
Atrooz, F., Alkadhi, K. A., & Salim, S. (2021) · Current Research in Neurobiology · doi:10.1016/j.crneur.2021.100013 · Cited by 213
Childhood Maltreatment and Psychopathology Affect Brain Development During Adolescence
Whittle, S., Dennison, M., Vijayakumar, N., Simmons, J. G., Yücel, M., Lubman, D. I., Pantelis, C., & Allen, N. B. (2013) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1016/j.jaac.2013.06.007 · Cited by 187
Nair, A., Vadodaria, K. C., Banerjee, S. B., Benekareddy, M., Dias, B. G., Duman, R. S., & Vaidya, V. A. (2007) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301276 · Cited by 189
Kalynchuk, L. E., Gregus, A., Boudreau, D., & Perrot-Sinal, T. S. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.6.1365 · Cited by 188
Mucha, M. W., Skrzypiec, A. E., Schiavon, E., Attwood, B. K., Kucerova, E., & Pawlak, R. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1107936108 · Cited by 191
The Role of the Forebrain Glucocorticoid Receptor in Acute and Chronic Stress
Furay, A. R., Packard, A. E. B., & Herman, J. P. (2008) · Endocrinology · doi:10.1210/en.2008-0642 · Cited by 189
Epigenetic Mechanisms in Learned Fear: Implications for PTSD
Zovkic, I. B., & Sweatt, J. D. (2012) · Neuropsychopharmacology · doi:10.1038/npp.2012.79 · Cited by 192
Li, Y.-F., Huang, Y., Amsdell, S. L., Xiao, L., O'Donnell, J. M., & Zhang, H.-T. (2009) · Neuropsychopharmacology · doi:10.1038/npp.2009.66 · Cited by 185
Chronic Stress Remodels Synapses in an Amygdala Circuit-Specific Manner
Zhang, J.-Y., Liu, T.-H., He, Y., Pan, H.-Q., Zhang, W.-H., Yin, X.-P., Tian, X.-L., Li, B.-M., Wang, X.-D., Holmes, A., et al. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2018.06.019 · Cited by 183
PTSD-related neuroimaging abnormalities in brain function, structure, and biochemistry
Harnett, N. G., Goodman, A. M., & Knight, D. C. (2020) · Experimental Neurology · doi:10.1016/j.expneurol.2020.113331 · Cited by 201
New perspectives in glutamate and anxiety
Riaza Bermudo-Soriano, C., Perez-Rodriguez, M. M., Vaquero-Lorenzo, C., & Baca-Garcia, E. (2012) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2011.04.010 · Cited by 207
Kleen, J. K., Sitomer, M. T., Killeen, P. R., & Conrad, C. D. (2006) · Behavioral Neuroscience · doi:10.1037/0735-7044.120.4.842 · Cited by 186
Molecular mechanisms of neuroplasticity and pharmacological implications: the example of tianeptine
McEwen, B. S., & Chattarji, S. (2004) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2004.09.008 · Cited by 174
Self-citationSturm, V. E., Yokoyama, J. S., Seeley, W. W., Kramer, J. H., Miller, B. L., & Rankin, K. P. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1301119110 · Cited by 181
A ghrelin-growth hormone axis drives stress-induced vulnerability to enhanced fear
Meyer, R. M., Burgos-Robles, A., Liu, E., Correia, S. S., & Goosens, K. A. (2014) · Molecular Psychiatry · doi:10.1038/mp.2013.135 · Cited by 169
The Neurobiology and Pharmacotherapy of Posttraumatic Stress Disorder
Abdallah, C. G., Averill, L. A., Akiki, T. J., Raza, M., Averill, C. L., Gomaa, H., Adikey, A., & Krystal, J. H. (2018) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-010818-021701 · Cited by 179
A neuroendocrine mechanism for sustaining fear
Schulkin, J. A., Morgan, M. A., & Rosen, J. B. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.09.009 · Cited by 177
Psychedelics and Other Psychoplastogens for Treating Mental Illness.
Vargas, M. V., Meyer, R., Avanes, A. A., Rus, M., & Olson, D. E. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.727117 · Cited by 166
Kosten, T. A., Galloway, M. P., Duman, R. S., Russell, D. S., & D'Sa, C. (2008) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301527 · Cited by 165
The ever‐changing brain: Cellular and molecular mechanisms for the effects of stressful experiences
McEwen, B. S. (2012) · Developmental Neurobiology · doi:10.1002/dneu.20968 · Cited by 165
Zoladz, P. R., Conrad, C. D., Fleshner, M., & Diamond, D. M. (2008) · Stress · doi:10.1080/10253890701768613 · Cited by 170
Microbiota regulates visceral pain in the mouse
Luczynski, P., Tramullas, M., Viola, M. F., Shanahan, F., Clarke, G. A., O’Mahony, S. M., Dinan, T. G., & Cryan, J. F. (2017) · eLife · doi:10.7554/elife.25887 · Cited by 174
Richardson, H. N., Zorrilla, E. P., Mandyam, C. D., & RIVIER, C. L. (2006) · Endocrinology · doi:10.1210/en.2005-1054 · Cited by 163
Bremner, J. D. (2006) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/187152706778559309 · Cited by 165
Chronic Stress Weakens Connectivity in the Prefrontal Cortex: Architectural and Molecular Changes.
Woo, E., Sansing, L. H., Arnsten, A. F. T., & Datta, D. (2021) · Chronic Stress · doi:10.1177/24705470211029254 · Cited by 159
Bottaccioli, A. G., Bottaccioli, F., & Minelli, A. (2018) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13728 · Cited by 173
Remodeling of axo-spinous synapses in the pathophysiology and treatment of depression
Licznerski, P., & Duman, R. S. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2012.09.057 · Cited by 157
Naert, G., IXART, G., Maurice, T., Tapia‐Arancibia, L., & Givalois, L. (2010) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2010.08.006 · Cited by 160
Corticosteroid-Induced Neural Remodeling Predicts Behavioral Vulnerability and Resilience
Gourley, S. L., Swanson, A. M., & Koleske, A. J. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2138-12.2013 · Cited by 156
Riva, G. (2011) · Journal of Diabetes Science and Technology · doi:10.1177/193229681100500213 · Cited by 159
Human amygdala development in the absence of species‐expected caregiving
Tottenham, N. (2012) · Developmental Psychobiology · doi:10.1002/dev.20531 · Cited by 149
Deconstructing the Gestalt: Mechanisms of Fear, Threat, and Trauma Memory Encoding
Maddox, S. A., Hartmann, J., Ross, R., & Ressler, K. J. (2019) · Neuron · doi:10.1016/j.neuron.2019.03.017 · Cited by 160
Veena, J., Srikumar, B. N., Raju, T. R., & Rao, B. S. S. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.03.059 · Cited by 161
Long-term consequences of childhood maltreatment: altered amygdala functional connectivity
Jedd, K., Hunt, R. H., Cicchetti, D., Hunt, E., Cowell, R. A., Rogosch, F. A., Toth, S. L., & Thomas, K. M. (2015) · Development and Psychopathology · doi:10.1017/s0954579415000954 · Cited by 149
Veena, J., Srikumar, B. N., Mahati, K., Bhagya, V. R., Raju, T. R., & Rao, B. S. S. (2008) · Journal of Neuroscience Research · doi:10.1002/jnr.21907 · Cited by 158
Wager‐Smith, K., & Markou, A. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.09.010 · Cited by 153
Chronic Stress- and Sex-Specific Neuromorphological and Functional Changes in Limbic Structures
McLaughlin, K. J., Baran, S. E., & Conrad, C. D. (2009) · Molecular Neurobiology · doi:10.1007/s12035-009-8079-7 · Cited by 158
Dissociation of the morphological correlates of stress‐induced anxiety and fear
Pêgo, J. M., Morgado, P. F., Pinto, L., Cerqueira, J., Almeida, O. F. X., & Sousa, N. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06112.x · Cited by 146
Animal models of post-traumatic stress disorder: face validity
Goswami, S., Rodríguez-Sierra, O. E., Cascardi, M. A., & Paré, D. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2013.00089 · Cited by 165
Soetanto, A., Wilson, R. S., Talbot, K., Un, A., Schneider, J. A., Sobiesk, M., Kelly, J., Leurgans, S., Bennett, D. A., & Arnold, S. E. (2010) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2010.48 · Cited by 148
Molecular and Cellular Mechanisms of Rapid-Acting Antidepressants Ketamine and Scopolamine
Wohleb, E. S., Gerhard, D. M., Thomas, A., & Duman, R. S. (2016) · Current Neuropharmacology · doi:10.2174/1570159x14666160309114549 · Cited by 151
Eiland, L. R., & McEwen, B. S. (2010) · Hippocampus · doi:10.1002/hipo.20862 · Cited by 148
The Clinical Implications Of Cognitive Impairment and Allostatic Load in Bipolar Disorder
Vieta, E., Popović, D., Rosa, A. R., Solé, B., Grande, I., Frey, B. N., Martínez‐Arán, A., Sánchez‐Moreno, J., Balanzá‐Martínez, V., Tabarés‐Seisdedos, R., et al. (2012) · European Psychiatry · doi:10.1016/j.eurpsy.2011.11.007 · Cited by 149
Titus, D. J., Rao, B. S. S., Halahalli, H. N., Ramkumar, K., Srikumar, B. N., Singh, S. B., Chattarji, S., & Raju, T. R. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2006.11.037 · Cited by 146
Self-citationStress-induced spine loss in the medial amygdala is mediated by tissue-plasminogen activator
Bennur, S., Rao, B. S. S., Pawlak, R., Strickland, S., McEwen, B. S., & Chattarji, S. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.08.075 · Cited by 145
Self-citationHercher, C., Turecki, G., & Mechawar, N. (2009) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2009.01.006 · Cited by 148
Stress and Anxiety Across the Lifespan: Structural Plasticity and Epigenetic Regulation
Hunter, R. G., & McEwen, B. S. (2013) · Epigenomics · doi:10.2217/epi.13.8 · Cited by 142
Hippocampus: Molecular, Cellular, and Circuit Features in Anxiety
Shi, H., Wang, S., Wang, X., Zhang, R.-X., & Zhu, L. (2023) · Neuroscience Bulletin · doi:10.1007/s12264-023-01020-1 · Cited by 151
Nijs, J., Loggia, M. L., Polli, A., Moens, M., Huysmans, E., Goudman, L., Meeus, M., Vanderweeën, L., Ickmans, K., & Clauw, D. J. (2017) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2017.1353603 · Cited by 156
Carim-Todd, L., Bath, K. G., Fulgenzi, G., Yanpallewar, S., Jing, D., Barrick, C. A., Becker, J., Buckley, H., Dorsey, S. G., Lee, F. S., et al. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.5060-08.2009 · Cited by 138
Are BDNF and glucocorticoid activities calibrated?
Jeanneteau, F. D., & Chao, M. V. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.09.017 · Cited by 150
Chronic stress-induced hippocampal dendritic retraction requires CA3 NMDA receptors
Christian, K. M., Miracle, A. D., Wellman, C. L., & Nakazawa, K. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2010.11.033 · Cited by 138
Acute and chronic restraint stress alter the incidence of social conflict in male rats
Wood, G. E., Young, L. T., Reagan, L. P., & McEwen, B. S. (2003) · Hormones and Behavior · doi:10.1016/s0018-506x(02)00026-0 · Cited by 141
The social brain: Neurobiological basis of affiliative behaviours and psychological well-being
Walker, S. C., & McGlone, F. P. (2013) · Neuropeptides · doi:10.1016/j.npep.2013.10.008 · Cited by 145
Barch, D. M., Pagliaccio, D., Belden, A. C., Harms, M. P., Gaffrey, M. S., Sylvester, C. M., Tillman, R., & Luby, J. L. (2016) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2015.15081014 · Cited by 139
Temporal Lobe Epilepsy and Psychiatric Comorbidity
Vinti, V., Dell’Isola, G. B., Tascini, G., Mencaroni, E., Cara, G. D., Striano, P., & Verrotti, A. (2021) · Frontiers in Neurology · doi:10.3389/fneur.2021.775781 · Cited by 143
Individual differences in recovery from traumatic fear
Holmes, A., & Singewald, N. (2012) · Trends in Neurosciences · doi:10.1016/j.tins.2012.11.003 · Cited by 147
Braga, M. F. M., Aroniadou‐Anderjaska, V., Manion, S. T., Hough, C. J., & Li, H. (2003) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300297 · Cited by 141
Nair, A. R., & Vaidya, V. A. (2006) · Journal of Biosciences · doi:10.1007/bf02704114 · Cited by 140
Brain-Derived Neurotrophic Factor in Amygdala-Dependent Learning
Rattiner, L. M., Davis, M. E., & Ressler, K. J. (2005) · The Neuroscientist · doi:10.1177/1073858404272255 · Cited by 141
NMDA Receptor Blockade Alters Stress-Induced Dendritic Remodeling in Medial Prefrontal Cortex
Martin, K. P., & Wellman, C. L. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhr021 · Cited by 138
Asan, E., Steinke, M. R., & Lesch, K. (2013) · Histochemistry and Cell Biology · doi:10.1007/s00418-013-1081-1 · Cited by 142
McNeal, N., Scotti, M.-A. L., Wardwell, J., Chandler, D. L., Bates, S. L., LaRocca, M., Trahanas, D. M., & Grippo, A. J. (2014) · Autonomic Neuroscience · doi:10.1016/j.autneu.2013.10.001 · Cited by 135
Joca, S. R. L., Ferreira, F. R., & Guimarães, F. S. (2007) · Stress · doi:10.1080/10253890701223130 · Cited by 139
Kuo, J. R., Kaloupek, D. G., & Woodward, S. H. (2012) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2012.73 · Cited by 136
Early Life Stress Effects on Glucocorticoid—BDNF Interplay in the Hippocampus
Daskalakis, N. P., de Kloet, E. R., Yehuda, R., Malaspina, D., & Kranz, T. M. (2015) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2015.00068 · Cited by 141
How age, sex and genotype shape the stress response
Novais, A., Monteiro, S., Roque, S., Correia‐Neves, M., & Sousa, N. (2016) · Neurobiology of Stress · doi:10.1016/j.ynstr.2016.11.004 · Cited by 152
Modulation of Different States of Anxiety-Like Behavior by Chronic Stress.
Vyas, A., & Chattarji, S. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.6.1450 · Cited by 136
Self-citationProtective Prevention Effects on the Association of Poverty With Brain Development
Brody, G. H., Gray, J. C., Yu, T., Barton, A. W., Beach, S. R. H., Galván, A., MacKillop, J., Windle, M., Chen, E., Miller, G. E., et al. (2017) · JAMA Pediatrics · doi:10.1001/jamapediatrics.2016.2988 · Cited by 135
Dynamic network connectivity: a new form of neuroplasticity
Arnsten, A. F. T., Paspalas, C. D., Gamo, N. J., Yang, Y., & Wang, M. (2010) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2010.05.003 · Cited by 160
Tuning synaptic transmission in the hippocampus by stress: the CRH system
Chen, Y., Andres, A. L., Frotscher, M., & Baram, T. Z. (2012) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2012.00013 · Cited by 136
Stress and the dynamic genome: Steroids, epigenetics, and the transposome
Hunter, R. G., Gagnidze, K., McEwen, B. S., & Pfaff, D. W. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1411260111 · Cited by 137
Stress-Induced Functional Alterations in Amygdala: Implications for Neuropsychiatric Diseases
Zhang, X., Ge, T., Yin, G., Cui, R., Zhao, G., & Yang, W. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00367 · Cited by 150
Franklin, T. B., & Perrot-Sinal, T. S. (2005) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2005.05.008 · Cited by 140
The emotional Stroop task and posttraumatic stress disorder: A meta-analysis
Cisler, J. M., Wolitzky-Taylor, K. B., Adams, T. G., Babson, K. A., Badour, C. L., & Willems, J. L. (2011) · Clinical Psychology Review · doi:10.1016/j.cpr.2011.03.007 · Cited by 151
Synaptic Plasticity, Metaplasticity and Depression
Vose, L. R., & Stanton, P. K. (2016) · Current Neuropharmacology · doi:10.2174/1570159x14666160202121111 · Cited by 131
Frontolimbic structural changes in borderline personality disorder
Minzenberg, M., Fan, J., New, A. S., Tang, C. Y., & Siever, L. J. (2007) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2007.07.015 · Cited by 127
Dwyer, J. M., & Duman, R. S. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.11.011 · Cited by 139
Neuner, F., Catani, C., Ruf, M., Schauer, E., Schauer, M., & Elbert, T. (2008) · Child and Adolescent Psychiatric Clinics of North America · doi:10.1016/j.chc.2008.03.001 · Cited by 130
Casey, B. J., Glatt, C. E., Tottenham, N., Soliman, F., Bath, K., Amso, D., Altemus, M., Pattwell, S., Jones, R., Levita, L., et al. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.03.081 · Cited by 129
Neurobiological and clinical effects of the antidepressant tianeptine
Kasper, S., & McEwen, B. S. (2008) · CNS Drugs · doi:10.2165/00023210-200822010-00002 · Cited by 302
Suzuki, T., Amata, M., Sakaue, G., Nishimura, S., Inoue, T., Shibata, M., & Mashimo, T. (2007) · Anesthesia & Analgesia · doi:10.1213/01.ane.0000261514.19946.66 · Cited by 131
Redefining neuroendocrinology: Epigenetics of brain-body communication over the life course
McEwen, B. S. (2018) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2017.11.001 · Cited by 129
Chronic stress alters inhibitory networks in the medial prefrontal cortex of adult mice
Gilabert-Juan, J., Castillo-Gomez, E., Guirado, R., Moltó, M. D., & Nacher, J. (2013) · Brain Structure and Function · doi:10.1007/s00429-012-0479-1 · Cited by 125
Cohodes, E. M., Kitt, E. R., Baskin-sommers, A. R., & Gee, D. G. (2020) · Developmental Psychobiology · doi:10.1002/dev.21969 · Cited by 133
Hammack, S. E., Roman, C. W., Lezak, K. R., Kocho-Schellenberg, M., Grimmig, B. A., Falls, W. A., Braas, K. M., & May, V. (2010) · Journal of Molecular Neuroscience · doi:10.1007/s12031-010-9364-7 · Cited by 129
Hill, M. N., Hillard, C. J., & McEwen, B. S. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhq280 · Cited by 136
Ganzel, B. L., Kim, P., Glover, G. H., & Temple, E. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2007.12.010 · Cited by 127
Wright, R. L., Lightner, E. N., Harman, J. S., Meijer, O. C., & Conrad, C. D. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04948.x · Cited by 133
Pattern Separation of Emotional Information in Hippocampal Dentate and CA3
Leal, S. L., Tighe, S. K., Jones, C. K., & Yassa, M. (2014) · Hippocampus · doi:10.1002/hipo.22298 · Cited by 123
Meta-analysis reveals a lack of sexual dimorphism in human amygdala volume
Marwha, D., Halari, M., & Eliot, L. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.12.021 · Cited by 127
Metadata
- Authors
- Vyas, A., Mitra, R., Shankaranarayana Rao, B. S., & Chattarji, S.
- Affiliations
- Tata Institute of Fundamental Research (IN)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2002-08-01
- Volume
- 22
- Issue
- 15
- Pages
- 6810-6818
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6758130
- OpenAlex
- W2136403062
- Semantic Scholar
- 587bd6bf61952d2c4d4fa8f4155737d79006655e
- Cited by
- 1,662
- References
- 51
- Citations by year
- 2026: 42 · 2025: 36 · 2024: 47 · 2023: 50 · 2022: 51 · 2021: 83 · 2020: 94 · 2019: 89 · 2018: 111 · 2017: 87 · 2016: 99 · 2015: 83 · 2014: 90 · 2013: 112 · 2012: 86
- FWCI
- 11.49
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Neuroscience (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Council of Scientific and Industrial Research, India
- Directorate for Biological Sciences
- National Centre for Biological Sciences
- Topics
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- chronic stress, dendritic remodeling, hippocampus, amygdala, restraint stress, chronic unpredictable mild stress, CA3 pyramidal cells, basolateral amygdala, stellate neurons, dendritic atrophy, dendritic branching, stress response, structural plasticity, anxiety-like behavior, emotionality, mood disorders
- MeSH terms
- Adrenal Glands, Amygdala, Animals, Anxiety, Body Weight, Chronic Disease, Dendrites, Disease Models, Animal, Hippocampus, Male, Neuronal Plasticity, Neurons, Organ Size, Restraint, Physical, Stress, Physiological, Rats, Wistar, Pyramidal Cells, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review